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titleSerious Product Events and Adverse Reactions - SPEAR

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to report Serious (Product) Events and Adverse Reactions – S(P)EARs – to the WMDA.

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To access the reporting system, you login with your email address and password. If you do not have a password, contact the WMDA office

Aim

  • To gain insight in the occurrence of serious events and adverse effects in relation to blood stem cell donation by unrelated donors and blood stem cell collection/processing from unrelated donors.

Purpose

  • To collect and

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  • analyse information on recipient and donor serious adverse events (SAE) and reactions which affect donors and/or products from all WMDA stem

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  • cell donor registries and cord blood banks.

  • To follow a rapid alert system for disseminating information on SAE/R to all members of the international community in contact with allogeneic donors and patients.

Warning
titleImportant note on Rapid Alerts

The SPEAR Committee reviews all reported incidents once a week.

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Quick links

If you have a rapid alert that needs to be shared with the community quickly, we urge you to submit it via the online reporting tool and to immediately send an e-mail to sear-spear@wmda.info or call us on: +31 88 505 7900.

In case of recall or big risks for future donations or transfusions a report can be submitted as a rapid alert. This includes, but is not limited to:

  • any prohibition or restriction imposed by the competent authority/health authorities of any country in which the stem cell product is provided or transplanted;
  • donor death;

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Info
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Link to annual reports overview (for WMDA members only)


Wmda button red
buttontextSPEAR Annual Reports
buttonlinkhttps://share.wmda.info/x/S4tOGg

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Info
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SPEAR rapid alerts

Find below the link to the public WMDA webpage, where you will find all rapid alerts sent out.


Wmdabutton
buttontextRapid Alerts
buttonlinkhttps://share.wmda.info/x/jYWAGg

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